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Lower risk Medical device recall · FDA · Published September 22, 2022

Hamilton C6 Ventilator Recall: Backlight Glitches May Cause Temporary Screen Blackout

Hamilton Medical recalls C6 ventilators with serial numbers starting 6093-9590 due to temporary screen blackouts. This may affect patient monitoring but does not cause injury.

🇺🇸 FDA recall #Z-0267-2023Medical deviceHamilton Medical ›
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Recalling firmHamilton Medical AGParc Industrial Vial 10 · Domat/Ems, Switzerland
✎ GovInfoNow plain-language explainer

What happened, in plain English

Hamilton Medical is recalling some C6 ventilators because their screens briefly go black for 2-3 seconds before returning to normal. This glitch could temporarily interfere with patient monitoring but does not pose a safety risk. Read more at govinfonow.com/recall/60031-hamilton-c6-ventilator-recall-backlight-glitches-may-cause-temporary-screen.

Source Summary by GovInfoNow · govinfonow.com/recall/60031-hamilton-c6-ventilator-recall-backlight-glitches-may-cause-temporary-screen · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0267-2023

Cite this page

“Hamilton C6 Ventilator Recall: Backlight Glitches May Cause Temporary Screen Blackout.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60031-hamilton-c6-ventilator-recall-backlight-glitches-may-cause-temporary-screen. Based on FDA recall #Z-0267-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0267-2023%22&limit=1).

Why it’s dangerous

The ventilator screen occasionally goes black for 2-3 seconds before briefly brightening again. This temporary malfunction does not cause injury but could potentially disrupt patient monitoring during critical moments.

Who’s affected

Owners of Hamilton C6 ventilators with specific serial numbers listed in the recall notice are affected. Patients using these ventilators are at minimal risk due to the temporary nature of the screen issue.

How to tell if you have this one

Check your Hamilton C6 ventilator's serial number against the list of affected numbers provided in the recall notice. The list includes specific serial numbers starting with 6093 through 9590.

  • Brand
    Hamilton Medical
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Serial Number

    Verify your ventilator's serial number against the list of affected numbers provided in the recall notice.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 23 states.

Alaska: nationwideAKMaine: nationwideMEVermont: nationwideVTNew Hampshire: nationwideNHWashington: named in the noticeWAIdaho: named in the noticeIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: nationwideMNIllinois: nationwideILWisconsin: named in the noticeWIMichigan: named in the noticeMINew York: named in the noticeNYRhode Island: nationwideRIMassachusetts: named in the noticeMAOregon: nationwideORNevada: named in the noticeNVWyoming: named in the noticeWYSouth Dakota: nationwideSDIowa: nationwideIAIndiana: named in the noticeINOhio: named in the noticeOHPennsylvania: named in the noticePANew Jersey: nationwideNJConnecticut: nationwideCTCalifornia: named in the noticeCAUtah: nationwideUTColorado: nationwideCONebraska: nationwideNEMissouri: named in the noticeMOKentucky: named in the noticeKYWest Virginia: named in the noticeWVVirginia: named in the noticeVAMaryland: nationwideMDDelaware: nationwideDEArizona: nationwideAZNew Mexico: named in the noticeNMKansas: named in the noticeKSArkansas: nationwideARTennessee: nationwideTNNorth Carolina: named in the noticeNCSouth Carolina: named in the noticeSCDistrict of Columbia: nationwideDCOklahoma: nationwideOKLouisiana: nationwideLAMississippi: nationwideMSAlabama: nationwideALGeorgia: named in the noticeGAHawaii: nationwideHITexas: named in the noticeTXFlorida: named in the noticeFLPuerto Rico: named in the noticePR

FDA distribution: “U.S. Nationwide distribution including in the states of CA, FL, GA, ID, IN, KS, KY, MA, MI, MO, NV, NM, NY, NC, OH, PA, Puerto Rico, SC, TX, VA, WA, WV, WI, and WY.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: California, Florida, Georgia, Idaho, Indiana, Kansas, Kentucky, Massachusetts, Michigan, Missouri, Nevada, New Mexico, New York, North Carolina, Ohio, Pennsylvania, Puerto Rico, South Carolina, Texas, Virginia, Washington, West Virginia, Wisconsin, Wyoming.

Recall timeline

FDA published this recall 2 months after the firm started it.

1. Firm started the recall: Sep 22, 202212. FDA classified it Class II: Nov 18, 202223. Published in FDA’s Enforcement Report: Nov 30, 202232022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Does this recall pose a safety risk?

No, the temporary screen blackouts do not cause injury. The hazard is minor and does not require immediate action.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-0267-2023 (September 22, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0267-2023 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA